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1-Bromo-4-fluorobenzene → 1-Benzyl-4-(4-fluorophenyl)piperazine

HRID 343
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인쇄 미리보기

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HRID 343 반응식
Fc1ccc(Br)cc1.c1ccc(CN2CCNCC2)cc1>CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21.Cc1ccccc1.[Na+].[Pd]>Fc1ccc(N2CCN(Cc3ccccc3)CC2)cc1
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참가 물질

7

반응물 2

HCID 99931-Bromo-4-fluorobenzeneHCID 759941-Benzylpiperazine

생성물 1

HCID 7631991-Benzyl-4-(4-fluorophenyl)piperazine수율 74.98%

시약·촉매·용매 4

HCID 23676156Sodium t-butoxide시약HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)촉매HCID 4144353Palladium (II) acetate촉매

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온도
50 °C

실험 절차

diacetoxypalladium (12.74 mg, 0.06 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (32.8 mg, 0.06 mmol) were suspended in toluene (0.5 mL) under N2. Heated to 50C for 30 min (microwave). sodium 2-methylpropan-2-olate (109 mg, 1.13 mmol) was suspended in toluene (0.500 mL) under N2. 1-benzylpiperazine (0.099 mL, 0.57 mmol) and 1-bromo-4-fluorobenzene (0.093 mL, 0.85 mmol) were added, followed by the catalyst solution. Heated to 100C for 2h in the microwave (high abs), then rt over night. The product was purified on silica (0-25% EtOAc/heptane) Yield: 1-benzyl-4-(4-fluorophenyl)piperazine (115 mg, 75.0 %)

출처 및 근거

ORD 기록
ord-8809d217cb404d41bb5809dd5f95b269
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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HCID 1140Toluene용매